JPH0742560B2 - High temperature spring manufacturing method - Google Patents

High temperature spring manufacturing method

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Publication number
JPH0742560B2
JPH0742560B2 JP59262843A JP26284384A JPH0742560B2 JP H0742560 B2 JPH0742560 B2 JP H0742560B2 JP 59262843 A JP59262843 A JP 59262843A JP 26284384 A JP26284384 A JP 26284384A JP H0742560 B2 JPH0742560 B2 JP H0742560B2
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JP
Japan
Prior art keywords
spring
strength
high temperature
alloy
weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP59262843A
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Japanese (ja)
Other versions
JPS61143567A (en
Inventor
光雄 河合
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Toshiba Corp
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Toshiba Corp
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Priority to JP59262843A priority Critical patent/JPH0742560B2/en
Publication of JPS61143567A publication Critical patent/JPS61143567A/en
Publication of JPH0742560B2 publication Critical patent/JPH0742560B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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  • Springs (AREA)

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、各種機械,機器などの高温で長時間使用され
る高温バネに関する。
Description: TECHNICAL FIELD The present invention relates to a high temperature spring that is used for a long time at high temperature in various machines and devices.

(従来の技術) 蒸気タービンやガスタービン、その他内燃機関などの高
温で長時間使用される各種機械,機器などには高温バネ
が使用されている。
(Prior Art) High-temperature springs are used in various machines and devices such as steam turbines, gas turbines, and other internal combustion engines that are used at high temperatures for a long time.

従来より使用されている高温バネは重量%で炭素0.1%
以下、硅素1%以下、マンガン1%以下、クロム10〜20
%、アルミニウム0.3〜1%、チタン2〜3%、ニオブ
0.5〜1.5%、鉄5〜10%、残部ニッケルよりなるNi基析
出強化合金の線材,棒材,板材などの所定のバネ形状に
成形後、時効処理したものである。
The high temperature springs used in the past are 0.1% carbon by weight%
Below, silicon 1% or less, manganese 1% or less, chromium 10-20
%, Aluminum 0.3-1%, titanium 2-3%, niobium
It is formed into a predetermined spring shape such as a wire rod, rod, plate, etc. of a Ni-based precipitation strengthening alloy consisting of 0.5 to 1.5%, iron 5 to 10% and the balance nickel, and then aged.

しかし、この従来のバネを高温で使用すると時間の経過
と共に、バネ強さがリラキゼーションにより急激に低下
し、常に一定のバネ強さを維持できず、設計段階で所定
幅の許容範囲を有する設計値の範囲内にバネ強さを長時
間維持できないという欠点がある。また、最近の熱効率
向上に伴う各種機械,機器の高温化や小形化に対してバ
ネ強さが小さいという欠点も有している。
However, when this conventional spring is used at a high temperature, the spring strength sharply decreases due to relaxation due to the passage of time, and it is not possible to always maintain a constant spring strength. There is a drawback that the spring strength cannot be maintained for a long time within the design value range. Further, there is a drawback that the spring strength is small with respect to the temperature rise and miniaturization of various machines and equipment due to the recent improvement in thermal efficiency.

(発明が解決しようとする課題) 本発明は、かかる従来の事情に鑑みて成されたもので、
従来の高温バネに比べバネ強さが強く、また使用中のリ
ラキゼーションによる変形およびバネ強さの低下が小さ
い、強度耐リラキゼーションに優れた高温バネの製造方
法を提供しようとするものである。
(Problems to be Solved by the Invention) The present invention has been made in view of such conventional circumstances.
The purpose of the present invention is to provide a method for manufacturing a high-temperature spring that has a stronger spring strength than conventional high-temperature springs and that is less likely to be deformed or relaxed due to relaxation during use and has excellent strength-relaxation resistance. is there.

(課題を解決するための手段と作用) 本発明は、バネ素材であるNi基析出強化合金の線材、棒
材あるいは板材を980℃以上で溶体化処理し、その金属
組織の過半を等軸晶とする工程と、バネ強さを所要の強
さ以上になるような形状に成形する工程と、高温バネの
使用状態の応力負荷加熱により使用時におけるバネの強
さの変化が小さい安定したバネ強さを付与する安定化処
理の工程とを経て製造されることを特徴とした高温バネ
の製造方法である。
(Means and Actions for Solving the Problems) The present invention is a solution of a Ni-based precipitation strengthening alloy wire material, a bar material, or a plate material, which is a spring material, at 980 ° C. or higher, and a majority of its metallographic structure is equiaxed. And the step of forming the spring strength into a shape that exceeds the required strength, and the stable spring strength with little change in spring strength during use due to stress load heating during use of the high temperature spring. The method for manufacturing a high temperature spring is characterized in that the high temperature spring is manufactured through a stabilization treatment process for imparting strength.

また、バネ素材が、重量パーセントで炭素0.1%以下、
硅素1%以下、マンガン1%以下、クロム10〜25%、ア
ルミニウム0.1〜1%、チタン0.1〜2%、ニオブ1.5〜
6%、鉄2〜25%、モリブデン2〜10%、残部ニッケル
よりなる合金で、かつ前述した各工程を経て成ることを
特徴とする高温バネの製造方法である。
In addition, the spring material is less than 0.1% carbon by weight,
Silicon 1% or less, Manganese 1% or less, Chromium 10-25%, Aluminum 0.1-1%, Titanium 0.1-2%, Niobium 1.5-
A method for manufacturing a high temperature spring, which is an alloy composed of 6%, iron 2 to 25%, molybdenum 2 to 10%, and balance nickel, and is formed through the above-mentioned steps.

ここで、本発明の各工程の限定理由について説明する。Here, the reason for limiting each step of the present invention will be described.

まず、バネ素材であるNi基析出強化合金の線材、棒材あ
るいは板材を980℃以上で溶体化処理し、その金属組織
の過半を等軸晶とする工程の理由は、熱間鍛造,熱間圧
延あるいは熱間伸線などの加工工程がそのほとんどであ
る場合は、耐リラキゼーション性が得られないためであ
る。なお、溶体化処理温度は溶体化処理の効果および金
属組織の過半を等軸晶とするためには980℃以上、望ま
しくは1000℃以上が良い。
First of all, the reason for the process of solution-treating a wire rod, rod or plate of Ni-based precipitation strengthening alloy, which is a spring material, at 980 ° C or higher, and making the majority of its metallographic structure equiaxed is hot forging, hot rolling This is because when most of the working processes such as rolling or hot drawing are not performed, relaxation resistance cannot be obtained. The solution treatment temperature is preferably 980 ° C. or higher, and more preferably 1000 ° C. or higher in order to achieve the solution treatment effect and to make the majority of the metal structure into equiaxed crystals.

また、そ溶体化処理後に、若干の冷間加工を加えても良
い。
Also, some cold working may be added after the solution treatment.

次に、バネ強さを所要の強さ以上になるような形状に成
形する工程の理由は、次の工程の安定化処理の工程によ
り所要のバネ強さおよび形状にするために必要な工程
で、最初から所要の形状にしておいた場合には安定化処
理による変形で、所定のバネ強さ,形状が得られないた
めである。
Next, the reason for the step of forming the spring strength into a shape that is equal to or greater than the required strength is that it is necessary to obtain the required spring strength and shape by the stabilization process in the next step. This is because, if the desired shape is set from the beginning, the predetermined spring strength and shape cannot be obtained by the deformation due to the stabilization process.

次に、高温バネの使用状態の応力負荷加熱により使用時
におけるバネ強さの変化が小さい安定したバネ強さを付
与する安定化処理の工程の理由は、所要のバネ強さと形
状および耐リラキゼーション性を付与するためである。
この安定化処理の工程がない場合には、高温で使用中に
バネ強さおよびバネ形状の変化が大きく、長時間安定し
たバネ強さを発揮する高温バネは得られない。
Next, the reason for the stabilization process is to provide stable spring strength with little change in spring strength during use due to stress load heating during use of the high-temperature spring. This is for imparting the zation property.
Without this stabilization process, the spring strength and spring shape change greatly during use at high temperatures, and a high temperature spring that exhibits stable spring strength for a long time cannot be obtained.

この安定化処理の工程は、所要の強さ以上のバネ強さと
した後、高温バネの使用状態の応力負荷加熱により、高
温バネのバネ強さを設計段階で設定される所定幅の許容
範囲を有する設計値までリラキゼーションにより低下さ
せることにより、バネ強さの変化が小さい安定したバネ
強さを得るのである。これは、この際の応力付加は使用
時と全く同一の応力を負荷する必要はない。
In this stabilization process, after setting the spring strength to the required strength or higher, the spring strength of the high-temperature spring is set to the allowable range of the predetermined width set at the design stage by heating the high-temperature spring under stress load. By lowering the design value to the designed value by relaxation, a stable spring strength with a small change in spring strength can be obtained. This means that the stress applied at this time does not need to be applied with the same stress as that during use.

ここで、高温バネの使用状態の応力負荷化熱とは、高温
バネはその用途により圧縮,引張あるいは曲げなど各種
の応力を負荷される状態で使用されるが、この意図する
高温バネが負荷される応力の状態と同様の圧縮,引張あ
るいは曲げを行った状態で加熱を行うことである。な
お、この加熱条件および応力は加熱温度,時間などによ
り適宜設定することができる。
Here, the stress-loading heat when the high-temperature spring is in use means that the high-temperature spring is used in a state in which various stresses such as compression, tension or bending are applied depending on its application. The heating is performed under the same compression, tension or bending as the stress condition. The heating conditions and stress can be set appropriately depending on the heating temperature, time, and the like.

なお、この安定化処理の工程は、時効処理の後に行うの
が望ましいが、時効処理を兼ねて行っても良い。
The stabilizing process is preferably performed after the aging treatment, but may also be performed as the aging treatment.

次に、バネ素材であるNi基析出強化合金の組成の限定理
由としては、線材、棒材あるいは板材などに加工できる
と共に、所要のバネ形状に容易に成形できることと、従
来の高温バネよりも優れた耐リラキゼーション性が得ら
れることによる。
Next, the reason for limiting the composition of the Ni-based precipitation strengthening alloy that is a spring material is that it can be processed into a wire rod, a rod material or a plate material, and that it can be easily formed into a required spring shape, which is superior to conventional high temperature springs. This is due to the fact that relaxation resistance is obtained.

以下に、好ましいNi基析出強化合金の組成の限定理由に
つい述べる。
The reasons for limiting the composition of the preferable Ni-based precipitation strengthened alloy will be described below.

炭素(C)は、合金中に固溶し強度を向上させるために
必要な元素である。しかし、多量の含有は炭化物が結晶
粒界に析出し、耐粒界腐食性や靭性を害するので、その
炭素の含有量は0.1重量%以下が好ましい。さらに好ま
しくは0.02〜0.06重量%程度である。
Carbon (C) is an element necessary for forming a solid solution in the alloy and improving the strength. However, when a large amount is contained, carbide precipitates at the grain boundaries and impairs intergranular corrosion resistance and toughness. Therefore, the carbon content is preferably 0.1% by weight or less. More preferably, it is about 0.02 to 0.06% by weight.

硅素(Si)は、溶解時に脱酸剤として添加する元素であ
る。しかし、多量の含有は靭性や加工性を害するので、
その硅素の含有量は1重量%以下が好ましい。さらに好
ましくは0.1〜0.6重量%程度である。
Silicon (Si) is an element added as a deoxidizing agent during dissolution. However, since a large content impairs toughness and workability,
The content of silicon is preferably 1% by weight or less. More preferably, it is about 0.1 to 0.6% by weight.

マンガン(Mn)は、溶解時に脱酸,脱硫剤として添加す
る元素である。しかし、多量に添加してもその効果が小
さくなるので、そのマンガンの含有量は0.1重量%以下
が好ましい。さらに好ましくは0.1〜0.5重量%程度であ
る。
Manganese (Mn) is an element added as a deoxidizing and desulfurizing agent during dissolution. However, even if added in a large amount, the effect becomes small, so that the manganese content is preferably 0.1% by weight or less. More preferably, it is about 0.1 to 0.5% by weight.

クロム(Cr)は、合金の強度や耐酸化性,耐食性を向上
させるために必要な元素である。しかし、その量があま
り少ないと効果が少なく、逆にあまりその量が多いと加
工性を害するので、そのクロムの含有量は10〜25重量%
が好ましい。さらに好ましくは15〜20重量%である。
Chromium (Cr) is an element necessary for improving the strength, oxidation resistance and corrosion resistance of the alloy. However, if the amount is too small, the effect is small, and conversely, if the amount is too large, the workability is impaired, so the content of chromium is 10 to 25% by weight.
Is preferred. It is more preferably 15 to 20% by weight.

アルミニウム(Al)は、ニッケルとの金属間化合物を生
成して合金中に析出し、合金の強度を向上させるために
必要な元素である。しかし、その量があまり少ないと効
果が少なく、逆にあまりその量が多いとチタンやニオブ
の含有量の兼ね合いもあるが加工性を害するので、その
アルミニウムの含有量は0.1〜1重量%が好ましい。さ
らに好ましくは0.2〜0.7重量%である。
Aluminum (Al) is an element necessary for improving the strength of the alloy by forming an intermetallic compound with nickel and depositing it in the alloy. However, if the amount is too small, the effect is small. On the other hand, if the amount is too large, the content of titanium or niobium may be compromised, but the workability is impaired. Therefore, the aluminum content is preferably 0.1 to 1% by weight. . More preferably, it is 0.2 to 0.7% by weight.

チタン(Ti)は、アルミニウムと同様にニッケルとの金
属間化合物を生成して合金の強度を向上させるために必
要な元素である。しかし、その量があまり少ないと効果
が少なく、逆にあまりその量が多いとアルミニウムやニ
オブの含有量の兼ね合いもあるが加工性を害するので、
そのチタンの含有量は0.1〜2重量%が好ましい。さら
に好ましくは、0.2〜2重量%である。
Titanium (Ti) is an element necessary to improve the strength of the alloy by forming an intermetallic compound with nickel, similar to aluminum. However, if the amount is too small, the effect is small, and conversely, if the amount is too large, the workability is impaired though there is a balance of the contents of aluminum and niobium.
The titanium content is preferably 0.1 to 2% by weight. More preferably, it is 0.2 to 2% by weight.

ニオブ(Nb)は、アルミニウムやチタンと同様にニッケ
ルと金属間化合物を生成して合金の耐磨耗性と強度を向
上させるために必要な元素である。しかし、その量があ
まり少ないと効果が少なく、逆にあまりその量が多いと
アルミニウムやチタンの含有量の兼ね合いもあるが加工
性を害するので、そのニオブの含有量は1.5〜6重量%
が好ましい。
Niobium (Nb) is an element necessary for improving the wear resistance and strength of the alloy by forming an intermetallic compound with nickel like aluminum and titanium. However, if the amount is too small, the effect is small. On the contrary, if the amount is too large, the content of aluminum and titanium may be compromised, but the workability is impaired. Therefore, the content of niobium is 1.5 to 6% by weight.
Is preferred.

鉄(Fe)は、合金の熱間加工性を向上させるのに必要な
元素である。しかし、その量があまり少ないと効果が少
なく、逆にあまりその量が多いと耐食性を害するので、
その鉄の含有量は2〜25重量%が好ましい。
Iron (Fe) is an element necessary for improving the hot workability of the alloy. However, if the amount is too small, the effect is small, and if the amount is too large, the corrosion resistance is impaired.
The iron content is preferably 2 to 25% by weight.

モリブデン(Mo)は、合金の強度を向上させると共に耐
食性を向上させるのに必要な元素である。しかし、その
量があまり少ないと効果が少なく、逆にあまりその量が
多いと加工性を害するため、そのモリブデンの含有量は
2〜10重量%が好ましい。(実施例) 実施例1 高周波誘導溶解炉を用いて、重量%でC:0.31%,Si:0.23
%,Mn:0.2%,Cr:18.4%,Fe:17.5%,Ti:0.77%,Al:0.43
%,Nb:5.4%,Mo:3.6%,残部Niより成る合金インゴット
を得た。
Molybdenum (Mo) is an element required to improve the strength of the alloy and the corrosion resistance. However, if the amount is too small, the effect is small, and conversely, if the amount is too large, the workability is impaired. Therefore, the content of molybdenum is preferably 2 to 10% by weight. (Example) Example 1 Using a high frequency induction melting furnace, C: 0.31% in weight% and Si: 0.23
%, Mn: 0.2%, Cr: 18.4%, Fe: 17.5%, Ti: 0.77%, Al: 0.43
%, Nb: 5.4%, Mo: 3.6%, the balance Ni was obtained.

次いで、このインゴットに熱間鍛造や伸線加工を施し、
直径1.4mmの線材とした。
Next, hot forging and wire drawing are applied to this ingot,
The wire rod has a diameter of 1.4 mm.

このようにして得た線材の一部を切出し、1020℃で30分
間加熱後急冷した後、冷間で伸線を行い直径1.2mmの線
材のした。
A part of the wire rod thus obtained was cut out, heated at 1020 ° C. for 30 minutes and then rapidly cooled, and then cold drawn to obtain a wire rod having a diameter of 1.2 mm.

引続き、この線材で中心径11mm,自由長21.5mm,有効巻数
4.5回,全巻数6.5回のコイルバネを成形した後、718℃
で8時間、621℃で8時間の時効処理を施すことにより
バネの強さを所要の強さ以上とした。
Continued, this wire rod has a center diameter of 11 mm, a free length of 21.5 mm, and an effective number of turns.
After forming a coil spring 4.5 times and 6.5 times in total, 718 ℃
The spring strength was made equal to or higher than the required strength by performing an aging treatment for 8 hours at 621 ° C. for 8 hours.

さらに、このコイルバネを圧縮してコイル長さを12mmと
した状態で700℃,25時間の安定化処理を施し試験に供し
た。なお、コイルバネの金属組織を観察した結果、双晶
が見られる等軸晶であった。
Further, this coil spring was compressed and subjected to a stabilization treatment at 700 ° C. for 25 hours in a state where the coil length was 12 mm, and the test was performed. As a result of observing the metal structure of the coil spring, it was an equiaxed crystal in which twins were seen.

比較例1 上記実施例1で用いた直径1.2mmの線材で、中心径11mm,
自由長20mm,有効巻数4.5回,全巻数6.5回のコイルバネ
を成形した後、718℃で8時間、621℃で8時間の時効処
理を施すことによりバネ強さを所要の強さ以上とした状
態、すなわち実施例1のコイルバネの安定化処理を行わ
ない状態で使用するコイルバネで試験に供した。
Comparative Example 1 The wire rod having a diameter of 1.2 mm used in the above Example 1 has a center diameter of 11 mm,
After forming a coil spring with a free length of 20 mm, an effective number of turns of 4.5, and a total number of turns of 6.5, aging treatment was performed at 718 ° C for 8 hours and 621 ° C for 8 hours to make the spring strength more than the required strength. That is, the coil spring of Example 1 was used for the test without the stabilization treatment.

比較例2 上記実施例1で用いて直性1.4mmの線材の一部を切出
し、954℃で1時間加熱後急冷した後、冷間で伸線を行
い直径1.2mmの線材とした。
Comparative Example 2 A wire having a diameter of 1.2 mm was cut by cutting out a part of the wire having a straightness of 1.4 mm used in Example 1 above, heating at 954 ° C. for 1 hour and then rapidly cooling.

次いで、この線材で中心径11mm,自由長21.5mm,有効巻数
4.5回,全巻数6.5回のコイルバネを成形した後、718℃
で8時間、621℃で8時間の時効処理を施こした。
Next, this wire rod has a center diameter of 11 mm, a free length of 21.5 mm, and an effective number of turns.
After forming a coil spring 4.5 times and 6.5 times in total, 718 ℃
8 hours and 621 ° C. for 8 hours.

さらに、このコイルバネを圧縮してコイル長さを12mmと
した状態で600℃,15時間の安定化処理を施し試験に供し
た。
Further, this coil spring was compressed and subjected to a stabilization treatment at 600 ° C. for 15 hours in a state where the coil length was 12 mm, and the test was performed.

比較例3 従来の高温バネ素材である重量%でC:0.06%,Si:0.13
%,Mn:0.62%,Cr:15.4%,Fe:7.2%,Ti:2.5%,Al:0.83
%,Nb:0.82%,残部Niより成る合金を高周波誘導溶解炉
により溶製し合金インゴットを得た。
Comparative Example 3 C: 0.06%, Si: 0.13 by weight% which is a conventional high temperature spring material.
%, Mn: 0.62%, Cr: 15.4%, Fe: 7.2%, Ti: 2.5%, Al: 0.83
%, Nb: 0.82%, balance Ni was melted in a high frequency induction melting furnace to obtain an alloy ingot.

次いで、このインゴットに熱間鍛造や伸線加工を施し、
直径1.4mmの線材のした。
Next, hot forging and wire drawing are applied to this ingot,
Made of wire with a diameter of 1.4 mm.

このようにして得た線材の一部を切出し、1093℃で30分
間加熱後急冷した後、冷間で伸線を行い直線1.2mmの線
材とした。
A part of the wire rod thus obtained was cut out, heated at 1093 ° C. for 30 minutes and then rapidly cooled, and then drawn cold to obtain a wire rod having a straight line of 1.2 mm.

引続き、この線材で中心径11mm,自由長20mm,有効巻数4.
5回,全巻数6.5回のコイルバネを成形した後、650℃で
5時間の時効処理を施こし試験に供した。
Continued, this wire rod has a center diameter of 11 mm, a free length of 20 mm, and an effective number of turns 4.
After forming the coil spring 5 times and the total number of turns 6.5 times, the coil spring was subjected to an aging treatment at 650 ° C. for 5 hours and subjected to the test.

試験は、前述した実施例1と比較例1〜3の圧縮コイル
バネを12mmに圧縮固定した状態で600℃および700℃の炉
中に装入し、所定時間加熱した後室温に取出し加重を取
り除いた後、バネの自由長とバネの長さを12mmに圧縮す
るに要する荷重を測定した。その試験結果を第1図およ
び第2図に示す。なお、バネの金属組織は等軸晶であっ
た。
In the test, the compression coil springs of Example 1 and Comparative Examples 1 to 3 described above were loaded into a furnace at 600 ° C. and 700 ° C. in a state of being compressed and fixed to 12 mm, heated for a predetermined time, taken out to room temperature, and the weight was removed. After that, the free length of the spring and the load required to compress the spring length to 12 mm were measured. The test results are shown in FIGS. 1 and 2. The metal structure of the spring was equiaxed.

第1図および第2図より明らかなように、本発明に係る
高強度,耐リラキゼーション性に優れた高温バネは、比
較例のバネに比較し、高温で長時間応力が加わった状態
で使用されてもコイル長さおよびバネ強さはほとんど変
化していない。具体的に説明すると、本発明の所要の強
さ以上のバネ強さを付与した後安定化処理を施した本発
明に係る実施例1は、設計段階で所定幅の許容範囲を有
するバネ強さの設計値の範囲内で長時間安定したバネ強
さを有しているのに対し、時効処理までは実施例1ど同
一の処理を施してはいるものの安定化処理を行っていな
い比較例1は急激にそのバネ強さが低下している。この
ように、安定化処理を行わずに高いバネ強さを付与した
状態のまま使用すると、バネ強さは使用時において急激
に低下するのであり、本発明のように、所要の強さ以上
のバネ強さを付与した後、安定化処理によりそのバネ強
さを設計値の範囲内まで低下させなければ長時間安定し
たバネ強さを得ることはできないのである。
As is clear from FIG. 1 and FIG. 2, the high-temperature spring according to the present invention, which has high strength and excellent relaxation resistance, is in a state in which stress is applied at high temperature for a long time as compared with the spring of the comparative example. Even when used, the coil length and spring strength have hardly changed. More specifically, the embodiment 1 according to the present invention, in which the spring strength equal to or higher than the required strength of the present invention is applied and then subjected to the stabilization process, is the spring strength having an allowable range of a predetermined width at the design stage. Comparative Example 1 which has a stable spring strength for a long time within the range of the design value of 1. Has a sharp decrease in its spring strength. In this way, if the spring strength is used in a state where high spring strength is imparted without performing the stabilization process, the spring strength sharply decreases at the time of use. After applying the spring strength, it is not possible to obtain a stable spring strength for a long time unless the spring strength is reduced to within the design value range by the stabilization process.

また、本発明において安定化処理により低下させるバネ
強さ、言い換えれば設計値の範囲内のバネ強さを最初か
ら得ていると、比較例2あるいは比較例3のようにバネ
強さが低下するだけであり、長時間安定したバネ強さを
得ることはできないのある。
Further, in the present invention, when the spring strength to be reduced by the stabilization process, in other words, the spring strength within the range of the design value is obtained from the beginning, the spring strength is reduced as in Comparative Example 2 or Comparative Example 3. Only, there is no way to get stable spring strength for a long time.

以上のように、本発明の高温バネの製造方法によりれた
高温バネは、優れた耐リラキゼーション性を有し、常に
一定のバネ強さを長時間保持できる工業上有用なバネで
あることが判る。
As described above, the high temperature spring produced by the method for producing a high temperature spring according to the present invention has excellent relaxation resistance and is an industrially useful spring that can always maintain a constant spring strength for a long time. I understand.

(発明の効果) 本発明の高温バネの製造方法は、従来の高温バネに比べ
バネ強さが強く、また使用中のリラキゼーションによる
変形およびバネ強さの低下が小さい、強度耐リラキゼー
ションに優れた高温バネを得ることができる。
(Effects of the Invention) The method for manufacturing a high temperature spring of the present invention has a strength higher than that of the conventional high temperature spring, and is less likely to be deformed by relaxation during use and to be reduced in spring strength. An excellent high temperature spring can be obtained.

【図面の簡単な説明】[Brief description of drawings]

第1図および第2図は、本発明に係る高強度,耐リラキ
ゼーション性に優れた高温バネおよび比較例の高温バネ
に加重を加えバネ長さ12mmに圧縮した状態で加熱した
後、加重を取り除いたときのバネの自由長とバネの長さ
を12mmに圧縮するに要する荷重を測定した試験結果を示
す特性図である。
FIG. 1 and FIG. 2 show that the high-temperature spring according to the present invention having excellent strength and relaxation resistance and the high-temperature spring of the comparative example were loaded with a load and heated to a spring length of 12 mm, and then heated. FIG. 7 is a characteristic diagram showing the test results of measuring the free length of the spring when removing the and the load required to compress the spring length to 12 mm.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】バネ素材であるNi基析出強化合金の線材、
棒材あるいは板材を980℃以上で溶体化処理し、その金
属組織の過半を等軸晶とする工程と、バネ強さを所要の
強さ以上になるような形状に成形する工程と、高温バネ
の使用状態の応力負荷加熱により使用時におけるバネ強
さの変化が小さい安定したバネ強さを付与する安定化処
理の工程とを経て製造されることを特徴とする高温バネ
の製造方法。
1. A wire rod of Ni-based precipitation strengthening alloy, which is a spring material,
A process in which a bar or plate is subjected to solution treatment at 980 ° C or higher to make the majority of the metallographic structure equiaxed, a process in which the spring strength exceeds the required strength, and a high temperature spring. The method for producing a high-temperature spring, characterized in that the high-temperature spring is produced through a stabilization treatment step of providing a stable spring strength with a small change in spring strength during use due to stress load heating in use.
【請求項2】バネ素材が、重量パーセントで炭素0.1%
以下、硅素1%以下、マンガン1%以下、クロム10〜25
%、アルミニウム0.1〜1%、チタン0.1〜2%、ニオブ
1.5〜6%、鉄2〜25%、モリブデン2〜10%、残部ニ
ッケルよりなる合金であることを特徴とする特許請求の
範囲第1項記載の高温バネの製造方法。
2. The spring material is 0.1% carbon by weight.
Below, silicon 1% or less, manganese 1% or less, chromium 10-25
%, Aluminum 0.1 to 1%, titanium 0.1 to 2%, niobium
The method of manufacturing a high temperature spring according to claim 1, wherein the alloy is an alloy composed of 1.5 to 6%, iron 2 to 25%, molybdenum 2 to 10%, and the balance nickel.
JP59262843A 1984-12-14 1984-12-14 High temperature spring manufacturing method Expired - Lifetime JPH0742560B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59262843A JPH0742560B2 (en) 1984-12-14 1984-12-14 High temperature spring manufacturing method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59262843A JPH0742560B2 (en) 1984-12-14 1984-12-14 High temperature spring manufacturing method

Publications (2)

Publication Number Publication Date
JPS61143567A JPS61143567A (en) 1986-07-01
JPH0742560B2 true JPH0742560B2 (en) 1995-05-10

Family

ID=17381386

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59262843A Expired - Lifetime JPH0742560B2 (en) 1984-12-14 1984-12-14 High temperature spring manufacturing method

Country Status (1)

Country Link
JP (1) JPH0742560B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000044950A1 (en) * 1999-01-28 2000-08-03 Sumitomo Electric Industries, Ltd. Heat-resistant alloy wire

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2559845B2 (en) * 1989-04-18 1996-12-04 三菱製鋼株式会社 Coil spring automatic manufacturing method and device
JP4277113B2 (en) 2002-02-27 2009-06-10 大同特殊鋼株式会社 Ni-base alloy for heat-resistant springs

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5877559A (en) * 1981-10-30 1983-05-10 Hitachi Ltd Manufacture of spring for nuclear reactor with superior stress corrosion cracking resistance
JPS58136736A (en) * 1982-02-08 1983-08-13 Hitachi Ltd Ni alloy member
JPS58174538A (en) * 1982-04-02 1983-10-13 Hitachi Ltd Ni-based alloy member and manufacture thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000044950A1 (en) * 1999-01-28 2000-08-03 Sumitomo Electric Industries, Ltd. Heat-resistant alloy wire

Also Published As

Publication number Publication date
JPS61143567A (en) 1986-07-01

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